Accretion history of large ribosomal subunits deduced from theoretical minimal RNA rings is congruent with histories derived from phylogenetic and structural methods

Gene. 2020 May 15:738:144436. doi: 10.1016/j.gene.2020.144436. Epub 2020 Feb 3.

Abstract

Accretions of tRNAs presumably formed the large complex ribosomal RNA structures. Similarities of tRNA secondary structures with rRNA secondary structures increase with the integration order of their cognate amino acid in the genetic code, indicating tRNA evolution towards rRNA-like structures. Here analyses rank secondary structure subelements of three large ribosomal RNAs (Prokaryota: Archaea: Thermus thermophilus; Bacteria: Escherichia coli; Eukaryota: Saccharomyces cerevisiae) in relation to their similarities with secondary structures formed by presumed proto-tRNAs, represented by 25 theoretical minimal RNA rings. These ranks are compared to those derived from two independent methods (ranks provide a relative evolutionary age to the rRNA substructure), (a) cladistic phylogenetic analyses and (b) 3D-crystallography where core subelements are presumed ancient and peripheral ones recent. Comparisons of rRNA secondary structure subelements with RNA ring secondary structures show congruence between ranks deduced by this method and both (a) and (b) (more with (a) than (b)), especially for RNA rings with predicted ancient cognate amino acid. Reconstruction of accretion histories of large rRNAs will gain from adequately integrating information from independent methods. Theoretical minimal RNA rings, sequences deterministically designed in silico according to specific coding constraints, might produce adequate scales for prebiotic and early life molecular evolution.

Keywords: Alignment-free evolutionary reconstructions; Cladistics; Homology; Stem-loop hairpins.

MeSH terms

  • Computer Simulation
  • Escherichia coli / genetics
  • Evolution, Molecular
  • Genetic Code
  • Nucleic Acid Conformation
  • Phylogeny
  • RNA / genetics
  • RNA, Ribosomal / genetics*
  • RNA, Ribosomal / physiology
  • RNA, Transfer / genetics*
  • RNA, Transfer / physiology
  • Ribosome Subunits, Large / genetics*
  • Ribosome Subunits, Large / metabolism
  • Saccharomyces cerevisiae / genetics
  • Thermus thermophilus / genetics

Substances

  • RNA, Ribosomal
  • RNA
  • RNA, Transfer